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The Effects of Surface Modification on the Speciation of Metal Ions Intercalated into Aluminosilicates

Published online by Cambridge University Press:  03 September 2012

Stephen R. Wasserman
Affiliation:
Chemistry Division, Argonne National Laboratory, 9700 S. Cass Ave., Argonne IL 60439.
Daniel M. Giaquinta
Affiliation:
Chemistry Division, Argonne National Laboratory, 9700 S. Cass Ave., Argonne IL 60439.
Steven E. Yuchs
Affiliation:
Chemistry Division, Argonne National Laboratory, 9700 S. Cass Ave., Argonne IL 60439.
L. Soderholm
Affiliation:
Chemistry Division, Argonne National Laboratory, 9700 S. Cass Ave., Argonne IL 60439.
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Abstract

The effect of the addition of an organic monolayer to the surface of a clay mineral on the speciation of metal ions intercalated into the clay interlayer is probed by X-ray absorption spectroscopy. The presence of the monolayer changes the surface of the clay from hydrophilic to hydrophobic. It inhibits the interlayer ions from exchanging freely into environmental water and reduces the leach rate of cations out of the clay by approximately a factor of 20. Significant changes are observed when these coated samples are treated under hydrothermal and thermal conditions. Reductions of uranium(VI), in the form of uranyl, and copper(II) ions occur. In addition, the uranium aggregates, forming small particles that appear similar to UO2. Comparable conglomeration occurs with lead cations and with the reduced copper species.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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References

REFERENCES

1. Grim, R. E., Clay Mineralogy, 2nd ed. (McGraw-Hill, New York, 1968).Google Scholar
2. Rabo, Jule A., Zeolite Chemistry and Catalysis (American Chemical Society, Washington, D. C, 1976).Google Scholar
3. Brindley, G. W. and Brown, G., “Crystal Structures of Clay Minerals and Their X-ray Identification,” (Mineralogical Society, London, 1980).Google Scholar
4. Tennakoon, D. T. B., Thomas, J. M., Tricker, M. J., and Williams, J. O., J. Chem. Soc. Dalton 1974, 22072211 (1974).Google Scholar
5. Wasserman, S. R., Anderson, K. B., Song, K., Yuchs, S. E. and Marshall, C. L., U. S. Patent Applied For.Google Scholar
6. Maoz, R. and Sagiv, J., J. Colloid Interface Sci. 100, 465496 (1984).Google Scholar
7. Wasserman, S. R., Tao, Y.-T., and Whitesides, G. M., Langmuir 5, 10741087 (1989).Google Scholar
8. Mustre de leon, J., Rehr, J. J., Zabinsky, S. I., and Albers, R. C., Phys. Rev. B44, 41464156(1991).Google Scholar
9. Hench, L. L., Clark, D. E., and Yen-Bower, E. L., Nucl. Chem. Waste Manag. 1, 5975 (1980).Google Scholar
10. Cotton, F. A. and Wilkinson, G., Advanced Inorganic Chemistry, 5th ed. (John Wiley and Sons, New York, 1988).Google Scholar
11. Wasserman, S. R. (unpublished).Google Scholar
12. Lytle, F. W., Greegor, R. B., and Panson, A. J., Phys. Rev. B 37 (4), 15501562 (1988).Google Scholar
13. Bard, A. J., Parsons, R., and Joseph, J., “Standard Potentials in Aqueous Solutions,” (Marcel Dekker, New York, 1985).Google Scholar